Senior Technical Product Manager - Bioinformatics

About Tempus AI Tempus is making precision medicine a reality by applying AI in healthcare, deriving insights from our expansive library of clinical data and molecular data. We enable physicians to make real-time, data-driven decisions to deliver personalized care and targeted therapies for patients through our analytical machine learning platform that uses the power of artificial intelligence in healthcare. We also work with partners to facilitate discovery, development, and delivery of optimized therapeutic options for patients through distinctive solution sets. Our mission is for each patient to benefit from the treatment of others who came before by providing the healthcare industry tools that learn as we gather more data. It’s About Time. For more information, visit tempus.com.

Tempus AI

Tempus AI, Inc. (NASDAQ: TEM) is a technology company leading the adoption of AI to advance precision medicine.

T

tempus.com

1,001-5,000 employees

Biotechnology Research

Chicago, IL

2015

Public Company

130k LinkedIn followers

Raised $2.8B

• With the advent of genomic sequencing, we can finally decode and process our
• genetic makeup. We now have more data than ever before but providers don't have
• the infrastructure or expertise to make sense of this data. We’re on a mission
• to connect an entire ecosystem to redefine how genomic data is used in clinical
• settings.
• We are looking for a highly motivated and capable technical product manager with
• extensive experience and interest in translational cancer research, diagnostic
• test development, and systems validation and verification. This position
• requires experience with diagnostic products, clinical regulatory requirements
• for software systems,and  algorithms development. Top candidates will also
• significant experience in regulated device development. This role will report to
• the head of Bioinformatics and support software  product development functions.
• Managing software development lifecycle processes.
• Engaging with the quality and regulatory team and supporting quality
• processes.
• Incident management: Promptly triage, coordinate, and manage the resolution
• of isues.
• Stakeholder support: Provide dedicated and responsive support to all
• stakeholders using the bioinformatics software.
• Feature request intake and prioritization: Collect, prioritize, and manage
• feature requests to guide software development.
• Interfacing with Product Managers of downstream engineering teams during
• implementation.
• Data contract management with downstream engineering teams.
• Documentation: Maintain comprehensive and up-to-date documentation for all
• bioinformatics software.

• Significant experience in medical device development and regulatory
• submission
• 2-4 years relevant experience in diagnostics product development
• Familiarity with US FDA and EU IVDR regulatory frameworks.
• A track record of successful submissions to US and international regulatory
• agencies
• Experience in cancer genetics, immunology, or molecular biology
• Experience working with next-generation sequencing data
• Self-driven and works well in interdisciplinary teams
• Experience with communicating insights and presenting concepts to a diverse
• audience
• The expected salary range may vary for other locations. Actual salary may vary
• based on qualifications and experience. Tempus offers a full range of benefits,
• which may include incentive compensation, restricted stock units, medical and
• other benefits depending on the position.

• Incentive compensation
• Restricted stock units
• Medical benefits